A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6544562



Internal ID20917801
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:46408046..46423933hg38UCSC Ensembl
chr21:47827960..47843847hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg3815888
hg1915888
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18204211
Samples
Known GenesPCNT
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6544562
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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